Matches in SemOpenAlex for { <https://semopenalex.org/work/W2917792967> ?p ?o ?g. }
- W2917792967 endingPage "2037" @default.
- W2917792967 startingPage "2032" @default.
- W2917792967 abstract "We previously studied the metabolomics, transcriptomics and proteomics of intestinal tissue of Hirschsprung disease (HSCR) patients; the results suggested that the expression of prostaglandin E2(PGE2), prostaglandin E receptor 2(PTGER2) and microsomal prostaglandin E synthase-1 (mPGES-1) notably increased in HSCR colon tissues. We already verified the differential expression of PGE2/EP2 in HSCR patients; therefore we investigate how mPGES-1 derived PGE2 affects the migration and the potential mechanism in cells, revealing the role of mPGES-1 derived PGE2 in the pathogenesis of Hirschsprung disease.SH-SY5Y and SK-N-BE2 cell lines were obtained from American Type Culture Collection (ATCC, USA). Prostaglandin E2 and its synthetase inhibitors were purchased from Med Chem Express (MCE, USA). Migration assays were performed with transwell and scratch assays. Cell proliferation was confirmed by CCK8 method. Flow cytometer was used to detect the cell cycle and cell apoptosis. The expressions of mRNA and protein of EP2, ARP2/3 were determined by qRT-PCR and western blot respectively. Immunofluorescence and confocal laser scanning microscopy were used to observe the morphology and function of cytoskeleton.MPGES-1 derived PGE2 decreased the relative expression of EP2 and ARP2/3 and caused damage to cytoskeleton. As to cell functions, PGE2 inhibited cell migration while having no effects on the proliferation, cell cycle and apoptosis. By adding mPGES-1 inhibitor MK886 the abnormal expression and damaged cell function were reversed.MPGES-1 derived PGE2 inhibits the cell migration by regulating ARP2/3 complex via prostaglandin E2 receptor. Potential mechanisms are the damage of cytoskeleton and related proteins leading to failure of cell polarize and migration. Here we thoroughly inquire the role mPGES-1 derived PGE2 plays in cell migration which might provide a new thinking in the investigation interrelated to the pathogenesis of HSCR." @default.
- W2917792967 created "2019-03-02" @default.
- W2917792967 creator A5004863693 @default.
- W2917792967 creator A5017970376 @default.
- W2917792967 creator A5020871478 @default.
- W2917792967 creator A5021169746 @default.
- W2917792967 creator A5034250958 @default.
- W2917792967 creator A5037197831 @default.
- W2917792967 creator A5047030483 @default.
- W2917792967 creator A5054175249 @default.
- W2917792967 date "2019-10-01" @default.
- W2917792967 modified "2023-09-24" @default.
- W2917792967 title "MPGES-1 derived PGE2 inhibits cell migration by regulating ARP2/3 in the pathogenesis of Hirschsprung disease" @default.
- W2917792967 cites W1427793766 @default.
- W2917792967 cites W1981664111 @default.
- W2917792967 cites W1988564036 @default.
- W2917792967 cites W1994460343 @default.
- W2917792967 cites W1995205013 @default.
- W2917792967 cites W2018192635 @default.
- W2917792967 cites W2019235974 @default.
- W2917792967 cites W2024713922 @default.
- W2917792967 cites W2059514736 @default.
- W2917792967 cites W2078817264 @default.
- W2917792967 cites W2084224490 @default.
- W2917792967 cites W2086253072 @default.
- W2917792967 cites W2104882581 @default.
- W2917792967 cites W2108806825 @default.
- W2917792967 cites W2115837720 @default.
- W2917792967 cites W2125326038 @default.
- W2917792967 cites W2130583261 @default.
- W2917792967 cites W2153975175 @default.
- W2917792967 cites W2161791526 @default.
- W2917792967 cites W2163455170 @default.
- W2917792967 cites W2167730388 @default.
- W2917792967 cites W2169952110 @default.
- W2917792967 cites W2171108123 @default.
- W2917792967 cites W2215965559 @default.
- W2917792967 cites W2234136362 @default.
- W2917792967 cites W2264853099 @default.
- W2917792967 cites W2299313456 @default.
- W2917792967 cites W2461268882 @default.
- W2917792967 cites W2527523198 @default.
- W2917792967 cites W2556839614 @default.
- W2917792967 cites W2605162336 @default.
- W2917792967 cites W2774074031 @default.
- W2917792967 cites W2777610758 @default.
- W2917792967 cites W2800195991 @default.
- W2917792967 cites W4210445361 @default.
- W2917792967 cites W958352729 @default.
- W2917792967 doi "https://doi.org/10.1016/j.jpedsurg.2019.01.001" @default.
- W2917792967 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30814036" @default.
- W2917792967 hasPublicationYear "2019" @default.
- W2917792967 type Work @default.
- W2917792967 sameAs 2917792967 @default.
- W2917792967 citedByCount "3" @default.
- W2917792967 countsByYear W29177929672021 @default.
- W2917792967 countsByYear W29177929672022 @default.
- W2917792967 crossrefType "journal-article" @default.
- W2917792967 hasAuthorship W2917792967A5004863693 @default.
- W2917792967 hasAuthorship W2917792967A5017970376 @default.
- W2917792967 hasAuthorship W2917792967A5020871478 @default.
- W2917792967 hasAuthorship W2917792967A5021169746 @default.
- W2917792967 hasAuthorship W2917792967A5034250958 @default.
- W2917792967 hasAuthorship W2917792967A5037197831 @default.
- W2917792967 hasAuthorship W2917792967A5047030483 @default.
- W2917792967 hasAuthorship W2917792967A5054175249 @default.
- W2917792967 hasConcept C104317684 @default.
- W2917792967 hasConcept C126322002 @default.
- W2917792967 hasConcept C137738243 @default.
- W2917792967 hasConcept C1491633281 @default.
- W2917792967 hasConcept C153911025 @default.
- W2917792967 hasConcept C170493617 @default.
- W2917792967 hasConcept C178592051 @default.
- W2917792967 hasConcept C190283241 @default.
- W2917792967 hasConcept C203014093 @default.
- W2917792967 hasConcept C2776415932 @default.
- W2917792967 hasConcept C2777956040 @default.
- W2917792967 hasConcept C2778938600 @default.
- W2917792967 hasConcept C2780942790 @default.
- W2917792967 hasConcept C29537977 @default.
- W2917792967 hasConcept C502942594 @default.
- W2917792967 hasConcept C553184892 @default.
- W2917792967 hasConcept C55493867 @default.
- W2917792967 hasConcept C62112901 @default.
- W2917792967 hasConcept C62478195 @default.
- W2917792967 hasConcept C71924100 @default.
- W2917792967 hasConcept C86803240 @default.
- W2917792967 hasConcept C95444343 @default.
- W2917792967 hasConceptScore W2917792967C104317684 @default.
- W2917792967 hasConceptScore W2917792967C126322002 @default.
- W2917792967 hasConceptScore W2917792967C137738243 @default.
- W2917792967 hasConceptScore W2917792967C1491633281 @default.
- W2917792967 hasConceptScore W2917792967C153911025 @default.
- W2917792967 hasConceptScore W2917792967C170493617 @default.
- W2917792967 hasConceptScore W2917792967C178592051 @default.
- W2917792967 hasConceptScore W2917792967C190283241 @default.
- W2917792967 hasConceptScore W2917792967C203014093 @default.
- W2917792967 hasConceptScore W2917792967C2776415932 @default.